rs146378852

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Species

Homo sapiens

Symbol

rs146378852

Category

Variant

Variant type

SNP

Overlaps

NDFIP1

Location

5:142140592

Nucleotide Change

T>C

Most Severe Consequence

• synonymous variant

See all consequences

HGVS.g name

• (GRCh38)5:142140592T>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000253814.6:c.525T>C
• RefSeq:NM_030571.4:c.525T>C

HGVS.p name

• ENSP00000253814:p.Asp175=
• NP_085048:p.Asp175=

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences